1433010-32-2

Basic information

• Product Name: tert-butyl 4-azidophenethylcarbamate
• Synonyms: tert-butyl 4-azidophenethylcarbamate
• CAS NO: 1433010-32-2
• Molecular Weight: 262.312
• Mol File: 1433010-32-2.mol

Chemical Properties

• CAS DataBase Reference: tert-butyl 4-azidophenethylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 4-azidophenethylcarbamate(1433010-32-2)
• EPA Substance Registry System: tert-butyl 4-azidophenethylcarbamate(1433010-32-2)

Safety Data

• Hazardous Substances Data: 1433010-32-2(Hazardous Substances Data)

Upstream product

• 94838-59-2 tert-butyl 4-aminophenethylcarbamate 
• 13472-00-9 p-Aminophenethylamine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 73918-56-6 4-Bromophenethylamine 
• 120157-97-3 t-butyl 2-(4-bromophenyl)ethylcarbamate 

Downstream Products

• 1433011-00-7 (3aS,4S,6R,6aR)-6-[6-amino-2-(4-azidophenethylamino)-9H-purin-9-yl]-N-ethyl-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carboxamide 
• 1433011-20-1 (2S,3S,4R,5R)-5-[6-amino-2-(4-azidophenethylamino)-9H-purin-9-yl]-N-ethyl-3,4-dihydroxytetrahydrofuran-2-carboxamide 

Relevant articles and documents

Solid-Phase Enrichment and Analysis of Azide-Labeled Natural Products: Fishing Downstream of Biochemical Pathways

Many methods have been devised over the decades to trace precursors of specific molecules in cellular environments as, for example, in biosynthesis studies. The advent of click chemistry has facilitated the powerful combination of tracing and at the same time sieving the highly complex metabolome for compounds derived from simple or complex starting materials, especially when the click reaction takes place on a solid support. While the principle of solid-phase click reactions has already been successfully applied for selective protein and peptide enrichment, the successful enrichment of much smaller primary and secondary metabolites, showing great structural diversity and undergoing many different biosynthetic steps, has seen only little development. For bacterial secondary metabolism, a far broader tolerance for "clickable" precursors was observed than in ribosomal proteinogenesis, thus making this method a surprisingly valuable tool for the tracking and discovery of compounds within the cellular biochemical network. The implementation of this method has led to the identification of several new compounds from the bacterial genera Photorhabdus and Xenorhabdus, clearly proving its power.

Synthesis and biological evaluation of indole-2-carboxamides bearing photoactivatable functionalities as novel allosteric modulators for the cannabinoid CB1 receptor

5-Chloro-3-ethyl-N-(4-(piperidin-1-yl)phenethyl)-1H-indole-2-carboxamide (ORG27569, 1) is a prototypical allosteric modulator for the cannabinoid CB1 receptor. Based on this indole-2-carboxamide scaffold, we designed and synthesized novel CB1 allosteric m

Synthesis of photoreactive 2-phenethylamine derivatives-synthesis of adenosine derivatives enabling functional analysis of adenosine receptors by photoaffinity labeling

2-Phenylethylamine is well known as a substructure of many biologically active compounds, and the synthesis of its photoreactive derivatives to allow the analysis of biological functions is reported. This allowed us to synthesise ligands for adenosine rec